JP3298759B2 - Conductive resin composition - Google Patents

Conductive resin composition

Info

Publication number
JP3298759B2
JP3298759B2 JP1068495A JP1068495A JP3298759B2 JP 3298759 B2 JP3298759 B2 JP 3298759B2 JP 1068495 A JP1068495 A JP 1068495A JP 1068495 A JP1068495 A JP 1068495A JP 3298759 B2 JP3298759 B2 JP 3298759B2
Authority
JP
Japan
Prior art keywords
resin
carbon black
weight
resin composition
styrene
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP1068495A
Other languages
Japanese (ja)
Other versions
JPH08199075A (en
Inventor
健志 宮川
美基雄 清水
健司 鍋田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Denka Co Ltd
Original Assignee
Denki Kagaku Kogyo KK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
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Application filed by Denki Kagaku Kogyo KK filed Critical Denki Kagaku Kogyo KK
Priority to JP1068495A priority Critical patent/JP3298759B2/en
Publication of JPH08199075A publication Critical patent/JPH08199075A/en
Application granted granted Critical
Publication of JP3298759B2 publication Critical patent/JP3298759B2/en
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  • Compositions Of Macromolecular Compounds (AREA)
  • Container, Conveyance, Adherence, Positioning, Of Wafer (AREA)
  • Non-Insulated Conductors (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、ポリフェニレンエーテ
ル系樹脂、ポリスチレン系樹脂又はABS系樹脂の少な
くとも1種類から選ばれた熱可塑性樹脂及びカーボンブ
ラックからなるIC包装用導電性樹脂組成物において、
この導電性樹脂組成物にスチレン−ジエンブロック共重
合体に水素添加した樹脂を含有させることにより、IC
等と接触時の摩耗によるカーボンブラック等の脱離が原
因となるIC等の汚染を著しく減少させたIC包装用導
電性樹脂組成物に関する。
The present invention relates to a conductive resin composition for IC packaging, comprising a thermoplastic resin selected from at least one of polyphenylene ether resin, polystyrene resin and ABS resin, and carbon black.
By adding a hydrogenated resin to the styrene-diene block copolymer to the conductive resin composition,
The present invention relates to a conductive resin composition for IC packaging in which contamination of an IC or the like due to detachment of carbon black or the like due to abrasion at the time of contact with the IC is significantly reduced.

【0002】[0002]

【従来技術】従来からICやICを用いた電子部品の包
装形態としてインジェクショントレー、真空成形トレ
ー、マガジン、エンボスキャリアテープなどが使用され
ており、これらの包装容器には静電気によるIC等の破
壊を防止するために(1)包装容器の表面に帯電防止剤
を塗布する方法、(2)導電性塗料を塗布する方法、
(3)帯電防止剤若しくは導電性フィラーを分散させる
方法等が実施されている。
2. Description of the Related Art Injection trays, vacuum forming trays, magazines, embossed carrier tapes, and the like have conventionally been used for packaging ICs and electronic components using ICs. (1) a method of applying an antistatic agent to the surface of a packaging container, (2) a method of applying a conductive paint,
(3) A method of dispersing an antistatic agent or a conductive filler or the like has been implemented.

【0003】しかしながら、(1)の方法は、塗布直後
は十分な帯電防止効果を示すが、長時間の使用により、
水分による流出、摩耗による帯電防止剤の脱離が生じ易
く安定した性能が得られない。また表面固有抵抗値も1
9〜1012Ω程度であり厳しい帯電防止効果を要求さ
れるICの包装には不適当である。(2)の方法は、製
造において塗布が不均一となり易くまた摩耗による剥が
れ落ちのため帯電防止効果を失いICを破壊すると共に
ICのリード部を汚染するという欠点がある。(3)の
方法においては帯電防止剤では、添加量が多量に必要の
ため樹脂の物性を低下させ、また表面固有抵抗値が湿度
により大きく影響され安定した性能が得られない。
[0003] However, the method (1) shows a sufficient antistatic effect immediately after coating, but the method (1),
The antistatic agent is likely to be detached due to outflow due to moisture and abrasion, and stable performance cannot be obtained. The surface resistivity is also 1
0 is unsuitable for 9 to 10 12 Omega about a and packaging of IC that requires strict antistatic effect. The method (2) has the drawbacks that the coating tends to be non-uniform in the manufacture, and the antistatic effect is lost due to peeling off due to abrasion, the IC is destroyed, and the lead of the IC is contaminated. In the method (3), a large amount of the antistatic agent is required, so that the physical properties of the resin are deteriorated, and the surface specific resistance value is greatly affected by humidity, so that stable performance cannot be obtained.

【0004】又、導電性フィラーとしては金属微粉末、
カーボンファイバー、カーボンブラックなどが挙げられ
る。この内金属微粉末及びカーボンファイバーは、少量
の添加で十分な導電性が得られるが成形性が著しく低下
し、また均一に分散させることが難しく、かつ成形品の
表面に樹脂成分のみのスキン層が出来易く安定した表面
固有抵抗値が得られにくい。これらに対しカーボンブラ
ックは混練条件等の検討により均一に分散させることが
可能であり、安定した表面固有抵抗値が得られ易いこと
から一般的に使用されているが、カーボンブラックを多
量に添加する必要が有るため流動性や成形性が低下する
現象があった。
As the conductive filler, fine metal powder,
Examples include carbon fiber and carbon black. Of these metal powders and carbon fibers, sufficient conductivity can be obtained with a small amount of addition, but the moldability is remarkably reduced, it is difficult to disperse uniformly, and the skin layer of only the resin component is formed on the surface of the molded product. And it is difficult to obtain a stable surface specific resistance value. On the other hand, carbon black is generally used because it can be uniformly dispersed by studying kneading conditions and the like, and a stable surface specific resistance value is easily obtained, but a large amount of carbon black is added. Due to the necessity, there was a phenomenon that the fluidity and the moldability were reduced.

【0005】従来、カーボンブラックを分散させる樹脂
としては、一般用としてポリ塩化ビニル系樹脂、ポリプ
ロピレン系樹脂、ポリエチレンテレフタレート系樹脂、
ポリスチレン系樹脂及びABS系樹脂が、また100℃
以上での耐熱用としてポリフェニレンエーテル系樹脂、
ポリカーボネート樹脂などが用いられている。これらの
樹脂の中で耐熱用としてはポリフェニレンエーテル系樹
脂が、一般用としてはポリスチレン系樹脂及びABS系
樹脂がカーボンブラックを多量に添加しても流動性や成
形性の著しい低下がなく、さらにコストの面でも優れて
いる。しかしながら、カーボンブラックを多量に添加し
た組成物の成形品は、摩耗により成形品の表面からカー
ボンブラックが脱離し易いという欠点があった。
Conventionally, as resins for dispersing carbon black, polyvinyl chloride resins, polypropylene resins, polyethylene terephthalate resins for general use,
Polystyrene resin and ABS resin, 100 ℃
Polyphenylene ether resin for heat resistance above,
Polycarbonate resin and the like are used. Among these resins, polyphenylene ether resins are used for heat resistance, and polystyrene resins and ABS resins for general use are not significantly reduced in fluidity and moldability even when a large amount of carbon black is added. Also excellent in terms of. However, a molded article of the composition containing a large amount of carbon black has a disadvantage that carbon black is easily detached from the surface of the molded article due to abrasion.

【0006】[0006]

【発明が解決しようとする課題】本発明は、かかる欠点
を解決するものであり、カーボンブラックを含有するポ
リフェニレンエーテル系樹脂、ポリスチレン系樹脂又は
ABS系樹脂組成物に、さらに、スチレン−ジエンブロ
ック共重合体に水素添加した樹脂を含有させることによ
り、該導電性樹脂組成物から成るIC包装用の成形品に
おいて、成形品とIC等との接触・摩耗が原因となるカ
ーボンブラック等の脱離によるIC等の汚染を著しく減
少させた導電性樹脂組成物を提供しようとするものであ
る。
SUMMARY OF THE INVENTION The present invention has been made to solve the above-mentioned drawbacks. The present invention relates to a polyphenylene ether-based resin, a polystyrene-based resin or an ABS-based resin composition containing carbon black, and a styrene-diene block copolymer. By adding a hydrogenated resin to the polymer, in a molded article for IC packaging made of the conductive resin composition, contact and abrasion between the molded article and the IC may cause desorption of carbon black or the like. An object of the present invention is to provide a conductive resin composition in which contamination such as IC is significantly reduced.

【0007】[0007]

【課題を解決するための手段】すなわち、本発明の第1
の発明は、(A)ポリフェニレンエーテル系樹脂、ポリ
スチレン系樹脂又はABS系樹脂の少なくとも1種類か
ら選ばれた熱可塑性樹脂、(B)カーボンブラック及び
(C)スチレン−ジエンブロック共重合体に水素添加し
た樹脂からなるIC包装用導電性樹脂組成物において、
(a)前記(A)熱可塑性樹脂100重量部に対し
(B)カーボンブラック5〜50重量部を含有し、か
つ、前記(A)熱可塑性樹脂と(B)カーボンブラック
の合計量100重量部に対し(C)スチレン−ジエンブ
ロック共重合体に水素添加した樹脂1〜30重量部を含
有してなり、かつ、(b)導電性樹脂組成物の表面固有
抵抗値が102 〜1010Ωであることを特徴とするIC
包装用導電性樹脂組成物である。本発明の第2の発明
は、(C)スチレン−ジエンブロック共重合体に水素添
加した樹脂のスチレン含有量が10〜80重量%である
ことを特徴とする第1の発明のIC包装用導電性樹脂組
成物。
That is, the first aspect of the present invention is as follows.
The invention of (1) relates to hydrogenation of (A) a thermoplastic resin selected from at least one of a polyphenylene ether resin, a polystyrene resin and an ABS resin, (B) carbon black and (C) a styrene-diene block copolymer. In the conductive resin composition for IC packaging consisting of the resin obtained,
(A) 100 parts by weight of the thermoplastic resin (A), 5 to 50 parts by weight of (B) carbon black, and 100 parts by weight of the total of (A) the thermoplastic resin and (B) carbon black (C) 1 to 30 parts by weight of a resin obtained by hydrogenating a styrene-diene block copolymer, and (b) the conductive resin composition has a surface specific resistance of 10 2 to 10 10 Ω. IC characterized in that:
It is a conductive resin composition for packaging. According to a second aspect of the present invention, there is provided the conductive material for IC packaging according to the first aspect, wherein the styrene content of the resin obtained by hydrogenating the (C) styrene-diene block copolymer is 10 to 80% by weight. Resin composition.

【0008】以下、本発明を更に詳細に説明する。本発
明においては、(A)ポリフェニレンエーテル系樹脂、
ポリスチレン系樹脂又はABS系樹脂の少なくとも1種
類から選ばれた熱可塑性樹脂が使用され、ポリフェニレ
ンエーテル系樹脂とはポリフェニレンエーテル樹脂とポ
リスチレン系樹脂を主成分とする樹脂をいい、ポリフェ
ニレンエーテル樹脂とポリスチレン系樹脂の合計量10
0重量部中のポリフェニレンエーテル樹脂の含有量は2
8〜86重量部が好ましく、28重量部未満ではポリフ
ェニレンエーテル系樹脂としての十分な力学特性が得ら
れず、86重量部を越えると流動性の低下により成形加
工が困難となる。該ポリフェニレンエーテル樹脂とは米
国特許3383435号に記載されているホモポリマー
或いは共重合体が示される。
Hereinafter, the present invention will be described in more detail. In the present invention, (A) a polyphenylene ether-based resin,
A thermoplastic resin selected from at least one of a polystyrene resin and an ABS resin is used, and the polyphenylene ether resin refers to a resin having a polyphenylene ether resin and a polystyrene resin as main components, and a polyphenylene ether resin and a polystyrene resin. Total amount of resin 10
The content of polyphenylene ether resin in 0 parts by weight is 2
The amount is preferably from 8 to 86 parts by weight, and if it is less than 28 parts by weight, sufficient mechanical properties as a polyphenylene ether-based resin cannot be obtained, and if it exceeds 86 parts by weight, the flowability is reduced and molding processing becomes difficult. The polyphenylene ether resin is a homopolymer or a copolymer described in U.S. Pat. No. 3,383,435.

【0009】本発明で使用するポリスチレン系樹脂とは
一般のポリスチレン樹脂又は耐衝撃性ポリスチレン樹脂
及びこれらの混合物を主成分とするものをいい、ABS
系樹脂とはアクリルニトリル−ブタジエン−スチレンの
三成分を主体とした共重合体を主成分とするものをい
う。
The polystyrene resin used in the present invention refers to a resin mainly composed of a general polystyrene resin or impact-resistant polystyrene resin and a mixture thereof.
The term "based resin" means a resin mainly composed of a copolymer mainly composed of three components of acrylonitrile-butadiene-styrene.

【0010】本発明で使用する(B)カーボンブラック
は、ファーネスブラック、チャンネルブラック、アセチ
レンブラック等であり、好ましくは比表面積が大きく、
樹脂への添加量が少量で高度の導電性が得られるもので
ある。例えば,S.C.F.(Super Condu
ctive Furnace)、E.C.F.(Ele
ctric Conductive Furnac
e)、ケッチェンブラック(ライオン−AKZO社製商
品名)及びアセチレンブラックである。カーボンブラッ
クの添加量は、表面固有抵抗値が102 〜1010Ωとす
ることのできる添加量であり、(A)熱可塑性樹脂10
0重量部に対し(B)カーボンブラック5〜50重量部
が好ましい。添加量が5重量部未満では十分な導電性が
得られず表面固有抵抗値が上昇してしまい、50重量部
を越えると樹脂との均一分散性が悪化し、成形加工が困
難となり、かつ、機械的強度等の特性値が低下してしま
う。また表面固有抵抗値が1010Ωを越えると十分な帯
電防止効果が得られず、102Ω未満では導電性がよす
ぎて電磁誘導や静電誘導などにより起電力が生じICを
破壊する恐れがある。
The carbon black (B) used in the present invention is furnace black, channel black, acetylene black or the like, and preferably has a large specific surface area.
High conductivity can be obtained with a small amount added to the resin. For example, C. F. (Super Condu
active Furnace); C. F. (Ele
tric Conductive Furnac
e), Ketjen Black (Lion-AKZO Corporation) and acetylene black. The amount of carbon black to be added is such that the surface specific resistance can be set to 10 2 Ω to 10 10 Ω.
The carbon black (B) is preferably 5 to 50 parts by weight with respect to 0 parts by weight. If the amount is less than 5 parts by weight, sufficient conductivity cannot be obtained and the surface resistivity increases, and if it exceeds 50 parts by weight, the uniform dispersibility with the resin is deteriorated, and molding processing becomes difficult, and Characteristic values such as mechanical strength are reduced. If the surface resistivity exceeds 10 10 Ω, sufficient antistatic effect cannot be obtained. If the surface resistivity is less than 10 2 Ω, electroconductivity is too high to generate electromotive force due to electromagnetic induction or electrostatic induction, and IC may be destroyed. There is.

【0011】本発明で使用する(C)スチレン−ジエン
ブロック共重合体に水素添加した樹脂は、スチレン−ジ
エンブロック共重合体に水素添加して得られるものであ
る。(C)スチレン−ジエンブロック共重合体に水素添
加した樹脂は、メルトフローインデックス(JIS−K
−7210に準じて測定)が、200℃、荷重5kgの
条件で0.1g/10分以上であり、この数値未満では
ポリフェニレンエーテル系樹脂、ポリスチレン系樹脂、
ABS系樹脂との混練が困難となり、良好な組成物が得
られない。また水素添加する前のスチレン−ジエンブロ
ック共重合体のジエンとしては、ブタジエン若しくはイ
ソプレンが好ましい。スチレン−ジエンブロック共重合
体の中のスチレン含有量は10〜80重量%であり、好
ましくは10〜50重量%である。スチレン−ジエンブ
ロック共重合体中のスチレン含有量が10重量%未満で
はポリフェニレンエーテル系樹脂、ポリスチレン系樹
脂、ABS系樹脂それぞれへの分散性が低下し機械的強
度の低下が生じてしまい、80重量%を越えるとカーボ
ンブラック等の脱落への改善効果が十分得られない。
The resin obtained by hydrogenating the styrene-diene block copolymer (C) used in the present invention is obtained by hydrogenating a styrene-diene block copolymer. (C) A resin obtained by hydrogenating a styrene-diene block copolymer has a melt flow index (JIS-K
Is less than 0.1 g / 10 min under the conditions of 200 ° C. and a load of 5 kg. If the value is less than this value, polyphenylene ether resin, polystyrene resin,
Kneading with an ABS resin becomes difficult, and a good composition cannot be obtained. As the diene of the styrene-diene block copolymer before hydrogenation, butadiene or isoprene is preferred. The styrene content in the styrene-diene block copolymer is 10 to 80% by weight, preferably 10 to 50% by weight. If the styrene content in the styrene-diene block copolymer is less than 10% by weight, the dispersibility in each of the polyphenylene ether-based resin, polystyrene-based resin and ABS-based resin is reduced, and the mechanical strength is reduced. %, The effect of improving the removal of carbon black or the like cannot be sufficiently obtained.

【0012】(C)スチレン−ジエンブロック共重合体
に水素添加した樹脂の添加量は、熱可塑性樹脂とカーボ
ンブラックの合計量100重量部に対して1〜30重量
部が好ましく、特に好ましくは3〜25重量部である。
添加量が1重量部未満ではその効果が不十分であり、3
0重量部を越えるとポリフェニレンエーテル系樹脂、ポ
リスチレン系樹脂、ABS系樹脂中における分散が不均
一となり引張弾性率の低下や破断点強度の低下が生じポ
リフェニレンエーテル系樹脂、ポリスチレン系樹脂、A
BS系樹脂本来の特性を損なってしまう。
(C) The amount of the hydrogenated resin added to the styrene-diene block copolymer is preferably 1 to 30 parts by weight, particularly preferably 3 to 30 parts by weight, per 100 parts by weight of the total amount of the thermoplastic resin and carbon black. 2525 parts by weight.
If the amount is less than 1 part by weight, the effect is insufficient.
If the amount exceeds 0 parts by weight, the dispersion in the polyphenylene ether-based resin, polystyrene-based resin, and ABS-based resin becomes non-uniform, resulting in a decrease in tensile modulus and a decrease in strength at break, resulting in polyphenylene ether-based resin, polystyrene-based resin, and A
The inherent properties of the BS resin are impaired.

【0013】本発明の導電性樹脂組成物は、十分な成形
加工性を維持するために、表面固有抵抗値が102 〜1
10Ωとなるようにカーボンブラックを充填した場合、
メルトフローインデックス(JIS−K−7210に準
じて測定)が、ポリフェニレンエーテル系樹脂に充填し
た場合は、230℃、荷重10kgの条件で、ポリスチ
レン系樹脂に充填した場合は、200℃、荷重5kgの
条件で、ABS系樹脂に充填した場合は、220℃、荷
重10kgの条件で、それぞれ、0.1g/10分以上
である。
The conductive resin composition of the present invention has a surface specific resistance of 10 2 to 1 in order to maintain sufficient moldability.
When carbon black is filled so as to be 0 10 Ω,
The melt flow index (measured according to JIS-K-7210) is 230 ° C. and a load of 10 kg when filled in a polyphenylene ether resin, and 200 ° C. and a load of 5 kg when filled in a polystyrene resin. In the case where the ABS resin is filled under the conditions, at a temperature of 220 ° C. and a load of 10 kg, each is 0.1 g / 10 min or more.

【0014】更に、本発明の導電性樹脂組成物には、必
要に応じて流動特性を改善するための滑剤、可塑剤、加
工助剤、成形品の力学特性を改善するための補強剤など
の各種添加剤や他の樹脂成分を添加することが可能であ
る。本発明において、樹脂等各種原材料を混練、ペレッ
ト化するにはバンバリーミキサー、押出機等の公知の方
法を用いることが可能である。
Further, the conductive resin composition of the present invention may contain, if necessary, a lubricant, a plasticizer, a processing aid, a reinforcing agent for improving the mechanical properties of a molded article, and the like. Various additives and other resin components can be added. In the present invention, a known method such as a Banbury mixer or an extruder can be used for kneading and pelletizing various raw materials such as a resin.

【0015】[0015]

【実施例】以下、本発明を実施例によりさらに詳細に説
明する。表1に、本発明にて使用した原料について示
す。 実施例1〜7 使用する原料を、表2に示す組成割合にて各々計量し、
高速混合機により均一に混合した後、φ45mmベント
式二軸押出機を用いて混練し、ストランドカット法によ
りペレット化した。次にペレット化した組成物を、サン
プルMはφ65mm押出機(L/D=28)を用い50
0mm幅のTダイにより厚さ500μmのシート状に成
形したもの、サンプルNはインジェクション成形機(1
00t)により厚さ1mm×120mm角のプレート状
及び引張測定用試験片形状に成形したものを評価用のサ
ンプルとした。評価結果を表4及び表5に示す。各実施
例においてはカーボンブラックの脱落は無かった。
The present invention will be described in more detail with reference to the following examples. Table 1 shows the raw materials used in the present invention. Examples 1 to 7 The raw materials to be used were weighed at the composition ratios shown in Table 2, respectively.
After uniformly mixing with a high-speed mixer, the mixture was kneaded using a φ45 mm vent-type twin-screw extruder, and pelletized by a strand cut method. Next, the pelletized composition was sampled by using a φ65 mm extruder (L / D = 28) for sample M.
Sample N was formed into a sheet having a thickness of 500 μm by a T-die having a width of 0 mm.
A sample for evaluation was formed into a plate having a thickness of 1 mm × 120 mm square and a test piece for tensile measurement according to 00t). The evaluation results are shown in Tables 4 and 5. In each of the examples, no carbon black was dropped.

【0016】比較例1〜4 実施例1と同様にして、使用する原料を、表3に示す組
成割合にて各々計量し、高速混合機により均一に混合し
た後、φ45mmベント式二軸押出機を用いて混練し、
ストランドカット法によりペレット化した。次にペレッ
ト化した組成物にてサンプルM及びサンプルNを作成し
評価した。各比較例においてはカーボンブラックの脱落
が確認された。
Comparative Examples 1 to 4 In the same manner as in Example 1, the raw materials to be used were weighed at the composition ratios shown in Table 3 and uniformly mixed by a high-speed mixer. Kneading using
Pellets were formed by a strand cut method. Next, samples M and N were prepared from the pelletized composition and evaluated. In each of the comparative examples, it was confirmed that carbon black had fallen.

【0017】[0017]

【表1】 [Table 1]

【0018】[0018]

【表2】 [Table 2]

【0019】[0019]

【表3】 [Table 3]

【0020】[0020]

【表4】 [Table 4]

【0021】[0021]

【表5】 [Table 5]

【0022】尚、各評価は次に示す方法によって行っ
た。 (1)表面固有抵抗 サンプルM及びNともにロレスター表面抵抗計(三菱油
化社製)により電極間を10mmとしサンプル中任意の
10点を測定し、その対数平均値を表面固有抵抗値とし
た。 (2)破断点強度、引張弾性率 JIS−K−7113に準拠しサンプルMについては2
号形試験片、サンプルNについては1号形試験片を引張
速度10mm/minで測定した。
Each evaluation was performed by the following method. (1) Surface specific resistance Both samples M and N were measured with a Loresta surface resistance meter (manufactured by Mitsubishi Yuka Co., Ltd.) to set the distance between the electrodes to 10 mm, and any 10 points in the sample were measured. (2) Breaking point strength and tensile modulus According to JIS-K-7113, for sample M, 2
As for the No. 1 test piece and the sample N, the No. 1 test piece was measured at a tensile speed of 10 mm / min.

【0023】(3)カーボン脱落の有無 各シート及びプレートサンプルの表面にQFP14mm
×20mm/64pinのICを100gの荷重で押し
付け、ストローク15mmで100往復させ、その後I
Cのリード部をマイクロスコープで観察。リード部にカ
ーボンブラック等黒色の付着物の有無で評価した。 (4)MFI 各実施例及び比較例のペレットについてJIS−721
0に準拠し測定を行った。
(3) Presence or absence of carbon detachment QFP 14 mm on the surface of each sheet and plate sample
× 20 mm / 64 pin IC is pressed with a load of 100 g and reciprocated 100 times with a stroke of 15 mm.
Observe the lead part of C with a microscope. Evaluation was made based on the presence or absence of black deposits such as carbon black on the lead portion. (4) MFI Pellets of Examples and Comparative Examples are JIS-721.
The measurement was performed according to 0.

【0024】[0024]

【発明の効果】以上説明したとおり、ポリフェニレンエ
ーテル系樹脂、ポリスチレン系樹脂又はABS系樹脂の
少なくとも1種類から選ばれた熱可塑性樹脂及びカーボ
ンブラックからなるIC包装用導電性樹脂組成物におい
て、この導電性樹脂組成物に、さらに、スチレン−ジエ
ンブロック共重合体に水素添加した樹脂を含有させるこ
とにより、IC等と接触時の摩耗によるカーボンブラッ
ク等の脱離が原因となるIC等の汚染を著しく減少させ
たIC包装用導電性樹脂組成物を得ることが可能とな
る。
As described above, in the conductive resin composition for IC packaging comprising carbon black and a thermoplastic resin selected from at least one of polyphenylene ether-based resin, polystyrene-based resin and ABS-based resin, The conductive resin composition further contains a hydrogenated resin in the styrene-diene block copolymer to significantly reduce contamination of ICs and the like caused by detachment of carbon black and the like due to abrasion at the time of contact with the ICs and the like. It is possible to obtain a reduced conductive resin composition for IC packaging.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI //(C08L 25/04 (C08L 25/04 53:02) 53:02) (C08L 55/02 (C08L 55/02 53:02) 53:02) (56)参考文献 特開 平4−288363(JP,A) 特開 平4−366165(JP,A) 特開 平6−240131(JP,A) 特開 平2−175754(JP,A) 特開 平5−78568(JP,A) 特開 平6−172633(JP,A) 特開 平7−150000(JP,A) 特開 平8−188710(JP,A) (58)調査した分野(Int.Cl.7,DB名) C08L 1/00 - 101/16 C08K 3/00 - 13/08 H01B 5/16 H01L 21/68 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification code FI // (C08L 25/04 (C08L 25/04 53:02) 53:02) (C08L 55/02 (C08L 55/02 53: 02) 53:02) (56) References JP-A-4-288363 (JP, A) JP-A-4-366165 (JP, A) JP-A-6-240131 (JP, A) JP-A-2-175754 (JP, A) JP-A-5-78568 (JP, A) JP-A-6-172633 (JP, A) JP-A-7-150000 (JP, A) JP-A 8-188710 (JP, A) ( 58) Field surveyed (Int.Cl. 7 , DB name) C08L 1/00-101/16 C08K 3/00-13/08 H01B 5/16 H01L 21/68

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】(A)ポリスチレン系樹脂又はABS系樹
脂の少なくとも1種類から選ばれた熱可塑性樹脂、
(B)カーボンブラック及び(C)スチレン−ジエンブ
ロック共重合体に水素添加した樹脂からなるIC包装用
導電性樹脂組成物において、(a)前記(A)熱可塑性
樹脂100重量部に対し(B)カーボンブラック5〜5
0重量部を含有し、かつ、前記(A)熱可塑性樹脂と
(B)カーボンブラックの合計量100重量部に対し
(C)スチレン−ジエンブロック共重合体に水素添加し
た樹脂1〜30重量部を含有してなり、かつ、(b)導
電性樹脂組成物の表面固有抵抗値が102〜1010Ωで
あることを特徴とするIC包装用導電性樹脂組成物。
(A) a thermoplastic resin selected from at least one of a polystyrene resin and an ABS resin,
In the conductive resin composition for IC packaging comprising a resin obtained by hydrogenating (B) carbon black and (C) a styrene-diene block copolymer, (A) 100 parts by weight of the thermoplastic resin (A) ) Carbon black 5-5
1 to 30 parts by weight of a resin containing (C) hydrogenated styrene-diene block copolymer based on 100 parts by weight of the total of (A) the thermoplastic resin and (B) carbon black. And (b) the conductive resin composition has a surface specific resistance of 10 2 to 10 10 Ω.
【請求項2】(C)スチレン−ジエンブロック共重合体
に水素添加した樹脂のスチレン含有量が10〜80重量
%であることを特徴とする請求項1記載のIC包装用導
電性樹脂組成物。
2. The conductive resin composition for IC packaging according to claim 1, wherein the styrene content of the resin obtained by hydrogenating the styrene-diene block copolymer (C) is 10 to 80% by weight. .
【請求項3】請求項1又は請求項2のIC包装用導電性
樹脂組成物からなるIC包装用のシート。
3. A sheet for IC packaging comprising the conductive resin composition for IC packaging according to claim 1.
【請求項4】請求項1又は請求項2のIC包装用導電性
樹脂組成物からなるIC包装用の成形品。
4. A molded article for IC packaging comprising the conductive resin composition for IC packaging according to claim 1.
JP1068495A 1995-01-26 1995-01-26 Conductive resin composition Expired - Lifetime JP3298759B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1068495A JP3298759B2 (en) 1995-01-26 1995-01-26 Conductive resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1068495A JP3298759B2 (en) 1995-01-26 1995-01-26 Conductive resin composition

Publications (2)

Publication Number Publication Date
JPH08199075A JPH08199075A (en) 1996-08-06
JP3298759B2 true JP3298759B2 (en) 2002-07-08

Family

ID=11757100

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1068495A Expired - Lifetime JP3298759B2 (en) 1995-01-26 1995-01-26 Conductive resin composition

Country Status (1)

Country Link
JP (1) JP3298759B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100502562B1 (en) * 2003-03-21 2005-07-20 서광석 allowance method for volume conductivity on tray

Also Published As

Publication number Publication date
JPH08199075A (en) 1996-08-06

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